Canonical Allele Identifier: PA2830122378
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1807286
ClinVar RCV Id: RCV002475243

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Lys415Asn
CA367398236
NM_033507.3:c.1245G>T
CA367398238
NM_033507.3:c.1245G>C